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Agree, a parameter such as
The latter gives you finer level control, but it would convoluted CLI options. The former is limited, but covers most use-cases. |
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One setup I have used in the past is to call a set number of peaks for different experiments (for example, binding of a TF in various conditions) and then comparing how those peaks overlap on genomic features. An option in MSPC to keep the 50000 top peaks as determined by the combined p-value would allow this quite easily.
I know this can be done by setting a very permissible threshold and then filtering the output files, but if there is a way to do this during normal MSPC runtime, it would avoid sorting a massive bed file to find the top peaks.
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